Canonical Allele Identifier: CA287323618
Gene: AIPL1 HGNC NCBI

Linked Data

dbSNP Id: rs545558458
gnomAD v3: 17-6425404-C-T
gnomAD v4: 17-6425404-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.6425404C>T , CM000679.2:g.6425404C>T GRCh38
NC_000017.10:g.6328724C>T , CM000679.1:g.6328724C>T GRCh37
NC_000017.9:g.6269448C>T NCBI36
NG_008474.1:g.14796G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381129.8:c.*56G>A MANE Select ENSP00000370521.3:n.*56G>A
ENST00000250087.9:c.*56G>A ENSP00000250087.5:n.*56G>A
ENST00000381128.2:c.*1083G>A ENSP00000370520.2:n.*1083G>A
ENST00000381129.7:c.*56G>A ENSP00000370521.3:n.*56G>A
ENST00000570466.5:c.*56G>A ENSP00000461287.1:n.*56G>A
ENST00000570584.5:c.251+8515G>A
ENST00000574506.5:c.*56G>A ENSP00000458456.1:n.*56G>A
ENST00000575265.5:c.*1182G>A ENSP00000459673.1:n.*1182G>A
ENST00000576776.5:c.*56G>A ENSP00000460827.1:n.*56G>A
ENST00000621374.4:c.*229G>A ENSP00000481337.1:n.*229G>A
NM_001033054.2:c.*56G>A NP_001028226.1:n.*56G>A
NM_001033055.2:c.*56G>A NP_001028227.1:n.*56G>A
NM_001285399.2:c.*56G>A NP_001272328.1:n.*56G>A
NM_001285400.2:c.*56G>A NP_001272329.1:n.*56G>A
NM_001285401.2:c.*56G>A NP_001272330.1:n.*56G>A
NM_001285402.1:c.*56G>A NP_001272331.1:n.*56G>A
NM_014336.4:c.*56G>A NP_055151.3:n.*56G>A
NM_001033054.3:c.*56G>A NP_001028226.1:n.*56G>A
NM_001033055.3:c.*56G>A NP_001028227.1:n.*56G>A
NM_001285399.3:c.*56G>A NP_001272328.1:n.*56G>A
NM_001285400.3:c.*56G>A NP_001272329.1:n.*56G>A
NM_001285401.3:c.*56G>A NP_001272330.1:n.*56G>A
NM_001285402.2:c.*56G>A NP_001272331.1:n.*56G>A
NM_001285403.3:c.*1182G>A NP_001272332.1:n.*1182G>A
NM_014336.5:c.*56G>A MANE Select NP_055151.3:n.*56G>A
NM_001285403.4:c.*1182G>A NP_001272332.1:n.*1182G>A